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生成 H1-PAX6 报告细胞系以纯化 PAX6 阳性神经干细胞/祖细胞。

Generation of H1 PAX6 reporter cells to purify PAX6 positive neural stem/progenitor cells.

机构信息

Department of Pathophysiology, Key Lab for Shock and Microcirculation Research of Guangdong, Southern Medical University, Guangzhou, 510515, PR China.

Key Laboratory of Regenerative Biology and Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, South China Institute for Stem Cell Biology and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, 510530, PR China.

出版信息

Biochem Biophys Res Commun. 2018 Aug 25;502(4):442-449. doi: 10.1016/j.bbrc.2018.05.163. Epub 2018 Jun 1.

DOI:10.1016/j.bbrc.2018.05.163
PMID:29807013
Abstract

Neural conversion from human pluripotent cells (hPSCs) is a potential therapy to neurological disease in the future. However, this is still limited by efficiency and stability of existed protocols used for neural induction from hPSCs. To overcome this obstacle, we developed a reporter system to screen PAX6 neural progenitor/stem cells using transcription activator like effector nuclease (TALEN). We found that knock-in 2 A-EGFP cassette into PAX6 exon of human embryonic stem cells H1 with TALEN-based homology recombination could establish PAX6 H1 reporter cell line fast and efficiently. This reporter cell line could differentiate into PAX6 and EGFP double positive neural progenitor/stem cells (NPCs/NSCs) after neural induction. Those PAX6 NPCs could be purified, expanded and specified to post-mitotic neurons in vitro efficiently. With this reporter cell line, we also screened out 1 NPC-specific microRNA, hsa-miR-99a-5p, and 3 ESCs-enriched miRNAs, hsa-miR-302c-5p, hsa-miR-512-3p and hsa-miR-518 b. In conclusion, the TALEN-based neural stem cell screening system is safe and efficient and could help researcher to acquire adequate and pure neural progenitor cells for further application.

摘要

从人类多能干细胞(hPSCs)进行神经转化是未来治疗神经疾病的一种潜在疗法。然而,这仍然受到用于从 hPSCs 诱导神经的现有方案的效率和稳定性的限制。为了克服这一障碍,我们开发了一种使用转录激活因子样效应物核酸酶(TALEN)筛选 PAX6 神经祖细胞/干细胞的报告系统。我们发现,使用基于 TALEN 的同源重组将 2A-EGFP 盒敲入人胚胎干细胞 H1 的 PAX6 外显子中,可以快速有效地建立 PAX6 H1 报告细胞系。该报告细胞系在神经诱导后可分化为 PAX6 和 EGFP 双阳性神经祖细胞/干细胞(NPCs/NSCs)。这些 PAX6 NPCs 可以在体外高效地被纯化、扩增和特化为有丝分裂后神经元。利用该报告细胞系,我们还筛选出了 1 种 NPC 特异性 microRNA,hsa-miR-99a-5p,和 3 种 ESCs 富集的 microRNA,hsa-miR-302c-5p、hsa-miR-512-3p 和 hsa-miR-518b。总之,基于 TALEN 的神经干细胞筛选系统安全且高效,可帮助研究人员获得足够且纯净的神经祖细胞,用于进一步应用。

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